We found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleWhole-exome re-sequencing in a family quartet identifies POP1 mutations as the cause of a novel skeletal dysplasia.AuthorsGlazov EA; Zankl A; Donskoi M; Kenna TJ; Thomas GP; Clark GR; Duncan EL; Brown MAPublicationPLoS genetics, 2011, Vol 7, Issue 3, pe1002027ISSN1553-7404Publication typearticleDOI10.1371/journal.pgen.1002027